Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
10211 to 10220 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10211
POU class 3 homeobox 2
BRN2, N-Oct3, OCT7, OTF-7, OTF7, POUF3, brn-2, oct-7
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cerebral amyloid angiopathy, Bipolar depression, Erectile dysfunction, Neurotic disorder, Obesity, Schizophrenia, Scoliosis, Substance abuse

10212
POU class 3 homeobox 3
BRN1, OTF8, SNIBFIS, brain-1, oct-8
Neurodevelopmental disorder, Developmental disability, Intellectual developmental disorder, Intellectual developmental disorder dysmorphic, Non-specific syndromic intellectual disability, Osteoarthritis

10213
POU class 3 homeobox 4
BRAIN-4, BRN-4, BRN4, DFN3, DFNX2, OCT-9, OTF-9, OTF9
Ayazi syndrome, Bipolar disorder, Choroideremia-deafness-obesity syndrome, Chromosome xq21 deletion syndrome, Congenital ear anomaly, Deafness, nonsyndromic sensorineural, mitochondrial, Deafness, x-linked, Hereditary hearing loss, Major depressive disorder, Hearing loss with stapes fixation, Schizophrenia, Scoliosis, X-linked nonsyndromic hearing loss, X-linked hearing loss with perilymphatic gusher, Xq21 microdeletion syndrome

10214
POU class 4 homeobox 1
ATITHS, BRN3A, Oct-T1, RDC-1, brn-3A
Ataxia with intention tremor and hypotonia, Cerebellar dysfunction with variable cognitive and behavioral abnormalities, Cervical dysplasia, Myeloid leukemia, Uterine disease, Uterine neoplasms

10215
POU class 4 homeobox 2
BRN3.2, BRN3B, Brn-3b
Oligodendroglioma

10216
POU class 4 homeobox 3
BRN3C, DFNA15, DFNA42, DFNA52
Isolated sensorineural deafness, Nonsyndromic hearing loss, Bell's palsy, Congenital sensorineural hearing loss, Deafness, Hearing impairment, Hereditary hearing loss, Migraine, Rheumatoid arthritis, Scoliosis

10217
POU class 5 homeobox 1
OCT3, OCT4, OCT4Borf1, OTF-3, OTF3, OTF4, Oct-3, Oct-4, Oct3/4
Amphetamine or sympathomimetic abuse, Carcinogenesis, Congenital heart disease, Crohn disease, Gestational trophoblastic disease, Glioma, Congenital heart defect, Inflammatory bowel disease, Membranous glomerulonephritis, Multiple myeloma, Prostate cancer, Psoriasis, Psoriatic arthritis, Rheumatoid arthritis, Stevens-johnson syndrome
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10218
POU class 5 homeobox 1B
OCT4-PG1, OCT4PG1, OTF3C, OTF3P1, POU5F1P1, POU5F1P4, POU5FLC20, POU5FLC8
Neoplasms, Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Colonic neoplasms, Colorectal adenoma, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Lung cancer, Non-hodgkins lymphoma
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10219
POU domain class 5, transcription factor 2
SPRM-1
Major depressive disorder

10220
POU class 6 homeobox 2
RPF-1, WT5, WTSL
Autism, Dupuytren contracture, Dyslexia, Glaucoma, Hypogonadotropic hypogonadism, Insomnia, Metabolic syndrome, Oligodendroglioma, Open angle glaucoma, Willis-ekbom disease, Schizophrenia, Diabetes mellitus type 2, Wilms tumor